Evidence map›Paper›PMID 32567084›Full record

ArticleCancer2020

Vitamin D intake is associated with decreased risk of immune checkpoint inhibitor-induced colitis.

Shilpa Grover, Michael Dougan, Kevin Tyan, Anita Giobbie-Hurder, Steven M Blum, Jeffrey Ishizuka, Taha Qazi, Rawad Elias, Kruti B Vora, Alex B Ruan and 11 more

Open access · bronzeAbstract read
In one paragraph

Article in Cancer, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed, 3 pooled it
5.4field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

43 citing papers in PubMed, 3 syntheses or guidelines pooled it, 68 citations in OpenAlex.

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  13. The Role of Vitamin D in Gastrointestinal Homeostasis and Gut Inflammation.International journal of molecular sciences · 2025
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

21 authors at 7 institutions in 1 country.

Shilpa GroverHarvard Medical School, Boston, Massachusetts.
Michael DouganHarvard Medical School, Boston, Massachusetts.
Kevin TyanHarvard Medical School, Boston, Massachusetts.ORCID 0000-0002-8585-1802
Anita Giobbie-HurderDivision of Biostatistics, Department of Data Sciences, Dana-Farber Cancer Institute, Boston, Massachusetts.
Steven M BlumHarvard Medical School, Boston, Massachusetts.
Jeffrey IshizukaDepartments of Medicine and Pathology, Yale University School of Medicine, New Haven, Connecticut.ORCID 0000-0002-4271-7312
Taha QaziDivision of Gastroenterology, Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts.
Rawad EliasHartford HealthCare Cancer Institute, Hartford, Connecticut.
Kruti B VoraHarvard Medical School, Boston, Massachusetts.
Alex B RuanHarvard Medical School, Boston, Massachusetts.
William Martin-DoyleHarvard Medical School, Boston, Massachusetts.
Michael ManosDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
Lauren EastmanDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
Meredith DavisDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
Maria GarganoDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
Rizwan HaqHarvard Medical School, Boston, Massachusetts.
Elizabeth I BuchbinderHarvard Medical School, Boston, Massachusetts.
Ryan J SullivanMassachusetts General Hospital Cancer Center, Boston, Massachusetts.
Patrick A OttHarvard Medical School, Boston, Massachusetts.
F Stephen HodiHarvard Medical School, Boston, Massachusetts.
Osama E RahmaHarvard Medical School, Boston, Massachusetts.
Harvard University · USDana-Farber Cancer Institute · USBrigham and Women's Hospital · USBroad Institute · USHartford Hospital · USMassachusetts General Hospital · USYale University · US

Funding

Training Program in Cancer Biology and TherapeuticsT32CA071345 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI Daniel A. Haber, Lecia V. Sequist · 1997 to 2026
$10.6M
Regulation of brown fat metabolism by the immune receptor PD-L1K08DK114563 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI DOUGAN, MICHAEL LAWRENCE · 2017 to 2021
$868k
American Gastroenterological AssociationMassachusetts General Hospital 2T32CA071345-21A1NCI NIH HHS T32 CA071345NIDDK NIH HHS 1K08 DK114563-01NIDDK NIH HHS K08 DK114563Parker Institute for Cancer Immunotherapy 5812101
6 · The paper itself

Abstract

backgroundThere is a lack of predictive markers informing on the risk of colitis in patients treated with immune checkpoint inhibitors (ICIs). The aim of this study was to identify potential factors associated with development of ICI colitis.

methodsWe performed a retrospective analysis of melanoma patients at Dana-Farber Cancer Institute who received PD-1, CTLA-4, or combination ICIs between May 2011 to October 2017. Clinical and laboratory characteristics associated with pathologically confirmed ICI colitis were evaluated using multivariable logistic regression analyses. External confirmation was performed on an independent cohort from Massachusetts General Hospital.

resultsThe discovery cohort included 213 patients of whom 37 developed ICI colitis (17%). Vitamin D use was recorded in 66/213 patients (31%) before starting ICIs. In multivariable regression analysis, vitamin D use conferred significantly reduced odds of developing ICI colitis (OR 0.35, 95% CI 0.1-0.9). These results were also demonstrated in the confirmatory cohort (OR 0.46, 95% CI 0.2-0.9) of 169 patients of whom 49 developed ICI colitis (29%). Pre-treatment neutrophil-to-lymphocyte ratio (NLR) ≥5 predicted reduced odds of colitis (OR 0.34, 95% CI 0.1-0.9) only in the discovery cohort.

conclusionsThis is the first study to report that among patients treated with ICIs, vitamin D intake is associated with reduced risk for ICI colitis. This finding is consistent with prior reports of prophylactic use of vitamin D in ulcerative colitis and graft-versus-host-disease. This observation should be validated prospectively in future studies.

Indexed as

AgedAntibodies, MonoclonalAntineoplastic Agents, ImmunologicalColitisCTLA-4 AntigenFemaleHumansImmune Checkpoint InhibitorsLymphocytesMaleMelanomaMiddle AgedNeutrophilsProgrammed Cell Death 1 ReceptorVitamin DAntibodies, MonoclonalAntineoplastic Agents, ImmunologicalCTLA-4 AntigenCTLA4 protein, humanImmune Checkpoint InhibitorsPDCD1 protein, humanProgrammed Cell Death 1 ReceptorVitamin DcolitisimmunotherapyirAEmelanomatoxicityvitamin D

Identifiers

PMID32567084
PMCPMC7381363
OpenAlexW3036937548

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.